Natural antibodie active against hiv virus

ABSTRACT

A preparation of human antibodies capable of neutralizing HIV-1 virus and the use thereof in the treatment of HIV infection.

[0001] The present invention relates to antibodies neutralizing the Human Immunodeficiency Virus. Said antibodies are present in sera from normal subjects and can be used to prevent the HIV infection or to delay the onset of illness in serum positive patients. The present invention further relates to pharmaceutical preparations containing said antibodies and the use thereof in passive immunotherapy of HIV infection.

BACKGROUND OF THE INVENTION

[0002] The induction of effective immune response to HIV-1 has often been restricted by the inability of any vaccine candidate to elicit antibodies capable of neutralizing infectivity of primary HIV isolates from infected individuals (1,2). On the other hand, from the analysis of sera from infected subjects resulted that neutralization of primary virus tends to be weak and sporadic (3,4). However, albeit it is difficult to raise antibodies, either during the infection or with experimental vaccines, monoclonal antibodies exist, such as IgG1b12, 2F5 and 2G12 (5-7), which are capable of neutralizing primary viruses of subtypes A-E. Said antibodies derive from subtype B—infected individuals and they are not raised by vaccination (8).

[0003] The earliest detectable HIV-1 specific antibody is of the IgG isotype (12), suggesting a nonconventional primary response (13). Furthermore, there are findings indicating that HIV-1 antigens react with pre-existing, antibody repertoires (14). Cross-reactive antibodies that recognize the HIV-1 envelope have been reported (15).

[0004] It was suggested that a strong early humoral response in HIV-1 infection may not be beneficial (16) as it would result in monoclonal and polyclonal antibody population instead of normal polyclonal response (13). It has been suggested that anti-idiotypic antibody 1F7 may broaden immune response to HIV antigens (17).

[0005] In our earlier studies, the homology of HIV envelope protein with IgG variable protein was predicted (18,19). However, recent data suggest that HIV-1 gp120 immunodominant epitope and a fraction of naturally-occurring IgG antibodies share complementary structure (20.21).

DISCLOSURE OF THE INVENTION

[0006] It has now been found that a group of antibodies present in sera from normal, not HIV—infected individuals, are capable of neutralizing HIV virus.

[0007] The antibody active fraction was purified from sera of normal subjects by affinity chromatography using a Sepharose resin to which total human IgG had been coupled. Observation evidenced that such anti-IgG antibodies fraction is capable of neutralizing HIV-1 infection in PBMC. The experiments were repeated using different anti-IgG preparations of various concentrations, obtained from commercial serum specimens, using affinity purified total IgG antibodies as negative control and HIVIG and mAb 4117C antibodies as positive control. The latter proved to be inactive to 92HT593B. Neutralization curves shown in FIG. 1 relate to a representative experiment carried out with HIV-1 primary isolates 92HT593B and SF162WT as well as with NLHX-ADA recombinant virus. Anti-IgG antibodies proved to be active against 92HT593B and NLHX-ADA at a 50% inhibiting concentration ranging from less than 1 to 7 μg/ml.

[0008] There is little possibility for the neutralizing effects observed with the preparation of anti-IgG antibodies to be due to co-purified chemokines from normal sera, as the concentration of these substances does not exceed 20 ng per ml of serum and no specific bands were revealed by PAGE. Furthermore, molecules below 50 kDa were removed by dialysis of the antibodies preparations. PAGE analysis of anti-IgG preparations revealed predominant presence of IgG and very small traces of contaminant proteins.

[0009] A possible explanation of the observed effects is that HIV-1 antigenic determinants share complementary structure with the variable regions of natural antibodies belonging to the immune network (9,23), but in no way this or other explanations limit the invention.

[0010] Therefore, a first aspect of the invention relates to a preparation of human antibodies raised against the total human IgG fraction, capable of neutralizing HIV-1. Said preparation can be obtained subjecting sera from normal, not HIV-infected subjects, to affinity chromatography using resins coupled to total human IgG fraction. The final concentration of isolated anti-IgG antibodies will be preferably comprised within the range of 0.1-1000 μg/ml, more preferably within the range of 0.11-100 μg/ml. The starting material consists of a pool of sera from normal subjects. According to a further aspect, the invention relates to the use of the preparation of the invention in the prophylactic or therapeutical treatment of HIV infection, preferably HIV-1 infection.

[0011] For the use in therapy, the preparation of the invention will be suitably formulated with pharmaceutically acceptable excipients. The latter include buffering agents, stabilizing agents, solubilizers, diluents, isotonicity agents and the like. The preparation will preferably be administered parenterally, preferably through the intravenous, intradermal or intramuscular route. According to a preferred embodiment, the preparation will be used in passive immunotherapy of HIV-1 infection.

DISCLOSURE OF THE FIGURES

[0012] FIG. 1

[0013] Neutralization of primary HIV-1 isolates SF162WT and 92HT593B and recombinant NL-HX-ADA virus by anti-IgG antibodies. Each titration curve represents data from a single experiment. Concentrations of anti-IgG in the various experiments were respectively 109.7, 12.3 and 80.0 μg/ml, for total IgG between 1000 and 3333 μg/ml and for HIVIG (10000 mg/ml). Anti-IgG and total IgG preparations were obtained as described in the following. HIVIG was prepared from sera of HIV-1 infected subjects.

[0014] FIG. 2

[0015] SDS-PAGE separation of affinity purified antibodies. Anti-IgG and total IgG antibodies were prepared as described below. Electrophoretic separation of anti-IgG antibodies revealed a prevalent content of IgG. In addition, although weak, bands of high molecular weight proteins were also present.

EXAMPLE 1 Preparation of Anti-IgG Antibodies

[0016] Anti-IgG antibodies were prepared from a pool of two normal human sera by affinity chromatography using Sepharose beads (CNBr-activated Sepharose 4B) to which total human IgG (purified on GammaBind Sepharose 4B affinity column) had previously been coupled. In principle, 5-7 mg of IgG antibodies/0.5-0.6 g of Sepharose beads were used. Binding was carried out following the indications of the manufacturer. The column was equilibrated with 5×PBS and heat-inactivated serum (1 ml) was loaded and diluted to 1:1 by 5×PBS. Incubation was carried out for 1 hour at room temperature or overnight at 4° C. After washing with 30 ml of 5×PBS, bound antibodies were eluted using 0.1 M citrate, pH=2.5 into test-tubes containing base-TRIS. The collected eluate was concentrated, dialyzed (Centricon YM, 30000 MW cut-off) and analyzed through 10% SDS-PAGE, predominantly revealing the IgG band (FIG. 2).

EXAMPLE 2 Neutralization of HIV-1 Isolates by Anti-IgG Antibodies

[0017] Virus neutralization was evaluated in PBMC following a previously published protocol (22). Neutralization assays were carried out with four different preparations of antibodies in five separated experiments.

[0018] Table 1 summarizes neutralization data against two HIV primary isolates (92HT593B, SF162WT) and a recombinant NL-HX-ADA virus.

[0019] HIVIG and mAb4117C were used as positive controls; Protein-G IgG was used as negative control.

[0020] In this test, all of the preparations of anti-IgG antibodies proved capable of inhibiting PBMC infection by 92HT593B and NL-HX-ADA, whereas no neutralizing activity against SF162WT was observed. TABLE Viral neutralization titers of purified Ig from sera from HIV-1 infected (a) and normal (b) subjects Recombinant Primary isolate virus Antibodies Preparat. 92HT593B SF162WT NLHX-ADA Assay μg/ml % neut μg/ml % neut μg/ml % neut. Negative control: Protein G IgG b) 150 8.3 150 2.9 150 −6.8 50 1.1 50 −0.5 50 −4.4 16.7 2.2 16.7 2.7 16.7 −4.4 Positive control: mAb4117C a) 100 16.1 100 100 100 98.7 33.3 9.0 33.3 100 33.3 96.0 11.1 5.2 11.1 100 1.1 55.0 3.7 0.4 3.7 80.4 3.7 23.2 1.2 −0.6 1.2 57.4 1.2 −8.6 Positivc control: HIVIG a) 100 88.0 100 57.4 100 93.4 33.3 62.0 33.3 39.9 33.3 94.8 11.1 44.4 11.1 2.1 11.1 92.4 3.7 39.4 3.7 −14.4 3.7 87.2 1.23 22.2 1.23 0.7 1.23 69.2 0.41 8.3 0.41 −3.7 0.41 54.5 Anti-IgG b) 1 1 1.87 57.4 NA ND 0.62 37.6 0.21 6.1 Anti-IgG b) 1 2 1.23 71.8 NA ND 0.41 48.9 0.14 14.4 Anti-IgG b) 2 1 8.00 42.0 NA 8.00 60.3 2.67 24.1 2.67 14.6 0.89 5.7 0.89 1.3 Anti-IgG b) 3 1 2.17 46.4 NA ND 0.72 27.1 0.24 3.3 Anti-IgG b) 4 1 10.97 39.8 NA 10.97 68.7 3.66 — 3.66 54.0 1.22 — 1.22 45.0

[0021] Literature

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1. Human antibodies aganist human IgG total fraction, capable of neutralizing HIV-1.
 2. Antibodies as claimed in claim 1, obtainable by subjecting sera from normal, non HIV-infected subjects, to affinity chromatography using resins bound to human IgG total fraction.
 3. Pharmaceutical preparation containing the antibodies of claims 1-2.
 4. The use of antibodies of claims 1 and 2 for the preparation of a medicament for use in the prevention or in the treatment of HIV infections.
 5. The use of antibodies of claims 1 and 2 for the preparation of a medicament for use in passive immunotherapy of HIV-1 infection. 